Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.75047266C>T | CA7275711 | MLH3 | c.2390G>A (p.Arg797His) n.2606G>A n.2553G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.75047266C>G | CA390440793 | MLH3 | c.2390G>C (p.Arg797Pro) n.2606G>C n.2553G>C | dbSNP |
14 | g.75047266C= | CA2147317549 | MLH3 | c.2390G= (p.Arg797=) n.2606G= n.2553G= | dbSNP |
14 | g.75047266C>A | CA390440794 | MLH3 | c.2390G>T (p.Arg797Leu) n.2606G>T n.2553G>T | dbSNP gnomAD v4 |